胰高血糖素样肽1受体激动剂(GLP-1RA)作为Semagulide(Rybelsus)对2型糖尿病(T2DM)的有效口服给药

H. Bando
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引用次数: 3

摘要

作为2型糖尿病(T2DM)的推荐药物,胰高血糖素样肽1受体激动剂(GLP-1Ra)因其各种有益作用而受到高度评价。其中,赛马鲁肽(Rybelsus)与有用的口服降血糖剂(OHA)在有用的口服形成方面一直备受关注。由于吸收促进剂N-(8-[2-羟基苯甲酰基]氨基)辛酸钠的开发技术,口服给药是可能的。一系列早期糖尿病治疗肽创新(PIONEER)显示了临床疗效,并充分减轻了体重和降低了HbA1c。从几个PIONER项目的结果来看,口服14 mg/天的赛马鲁肽使HbA1c值降低了约1.0-1.4%。
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Useful Oral Administration of Glucagon-Like Peptide 1 Receptor Agonist (GLP-1RA) as Semaglutide (Rybelsus) for Type 2 Diabetes Mellitus (T2DM)
As recommended pharmacological agents for type 2 diabetes mellitus (T2DM), Glucagon-Like Peptide 1 receptor agonist (GLP-1Ra) is highly evaluated for its various beneficial effects. Among them, semaglutide (Rybelsus) has been in focus for useful oral formation with useful oral hypoglycemic agent (OHA). Administration per os is possible due to the developed technique of absorption enhancer sodium N-(8-[2-hydroxybenzoyl] amino) caprylate. Clinical efficacy was shown by a series of Peptide Innovation for Early Diabetes Treatment (PIONEER) with enough weight reduction and decreased HbA1c. From the results of several PIONEER programs, oral semaglutide 14 mg/day had reduced HbA1c values by approximately 1.0-1.4%.
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